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PMID: 15109306 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Control of expression of the lectin-like protein Reg-1 by gastrin: role of the Rho family GTPase RhoA and a C-rich promoter element.

The Biochemical journal ·Vol. 381 ·No. Pt 2 ·2004-07-15 ·Pages 397-403

Ashcroft FJ, Varro A, Dimaline R, Dockray GJ

Abstract

The expression of members of the Reg family of secreted lectin-like proteins is increased in response to stress, inflammation and damage in many tissues. In the stomach, Reg is located in enterochromaffin-like cells, where its expression is stimulated by the gastric hormone gastrin. We have examined the mechanisms by which gastrin stimulates expression of Reg-1. Deletional mutations of 2.1 to 0.1 kb of the rat Reg-1 promoter in a luciferase reporter vector were transiently transfected into gastric cancer AGS-G(R) cells. All promoter fragments tested showed similar relative increases in luciferase expression in response to gastrin (1 nM). The response to gastrin of the smallest (104 bp) construct was 4.2+/-0.4-fold over basal. These responses were reduced by Ro-32-0432, a protein kinase C inhibitor, by C3-transferase, a Clostridium botulinum toxin and a selective inhibitor of the Rho family GTPase RhoA, and by co-transfection with a dominant negative form of RhoA. Co-transfection with a constitutively active form of RhoA stimulated expression 11.6+/-1.7-fold over basal. Mutations through the 104 bp construct identified a C-rich element (C-79CCCTCCC-72) required for responses to gastrin, PKC (protein kinase C) and L63RhoA (the constitutively active form of human RhoA protein containing a glutamine-to-leucine substitution at position 63). EMSAs (electrophoretic-mobility-shift assays) using nuclear extracts of control and gastrin-stimulated AGS-G(R) cells and a probe spanning -86 to -64 bp revealed multiple binding proteins. There was no effect of gastrin on the pattern of binding. Supershift assays indicated that transcription factors Sp1 and Sp3 bound the C-rich sequence. We conclude that gastrin stimulates Reg expression via activation of PKC and RhoA, that a C-rich region (-79 to -72) is critical for the response and that Sp-family transcription factors bind to this region of the promoter.

MeSH Terms
Animals Base Sequence/genetics,physiology Binding Sites/genetics,physiology Cytokines/metabolism Cytosine/metabolism DNA-Binding Proteins/physiology Enzyme Activation/physiology Gastrins/physiology Gene Expression Regulation/physiology Humans Luciferases/genetics Membrane Proteins/genetics Nerve Tissue Proteins/genetics Promoter Regions, Genetic/genetics,physiology Protein Kinase C/physiology Rats Recombinant Fusion Proteins/genetics Sequence Deletion/genetics,physiology Sp1 Transcription Factor/physiology Sp3 Transcription Factor Stomach Neoplasms Transcription Factors/physiology rhoA GTP-Binding Protein/physiology
Chemicals
Cytokines DNA-Binding Proteins Gastrins Membrane Proteins Nerve Tissue Proteins Recombinant Fusion Proteins SP3 protein, human Sp1 Transcription Factor Sp3 protein, rat Transcription Factors flotillins Sp3 Transcription Factor Cytosine Luciferases Protein Kinase C rhoA GTP-Binding Protein
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Ashcroft Felicity J
Physiological Laboratory, University of Liverpool, Crown Street, Liverpool L69 3BX, U.K.
Varro Andrea
Dimaline Rod
Dockray Graham J
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Article Info
Journal
The Biochemical journal
Abbr.
Biochem J
ISSN
1470-8728
Published
2004-07-15
Pages
397-403
Language
English
Region
England
NLM ID
2984726R
PMCID
PMC1133845
Subset
IM
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